234422006: Acute intermittent porphyria (disorder)

SNOMED CT Concept\constatation clinique\Disease\...

\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Acute intermittent porphyria

\trouble métabolique\Chronic metabolic disorder\Acute intermittent porphyria
\trouble métabolique\Disorder of porphyrin metabolism\Porphyria (disorder)\Acute intermittent porphyria
\trouble métabolique\Disorder of porphyrin metabolism\Porphobilinogen deaminase deficiency\Acute intermittent porphyria

\maladie chronique\Chronic metabolic disorder\Acute intermittent porphyria

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

351223014 Acute intermittent porphyria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

351224015 AIP - Acute intermittent porphyria en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

351225019 Pyrroloporphyria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

351226018 Acute porphyria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

351227010 Intermittent acute porphyria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

351228017 Swedish porphyria en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

351229013 Intermittent acute porphyria syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

547931000241118 porphyrie aigüe intermittente (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

622738015 Acute intermittent porphyria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

945791000172110 porphyrie aigüe intermittente fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Acute intermittent porphyria	est un(e) (attribut)	Chronic metabolic disorder	true	Inferred relationship	Some
Acute intermittent porphyria	Course	Intermittent	false	Inferred relationship	Some
Acute intermittent porphyria	est un(e) (attribut)	Porphyria (disorder)	true	Inferred relationship	Some
Acute intermittent porphyria	évolution clinique (attribut)	Intermittent	true	Inferred relationship	Some	1
Acute intermittent porphyria	est un(e) (attribut)	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Acute intermittent porphyria	est un(e) (attribut)	Porphobilinogen deaminase deficiency	true	Inferred relationship	Some
Acute intermittent porphyria	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
Acute intermittent porphyria	survenue (attribut)	congénital	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Homozygous acute intermittent porphyria	est un(e) (attribut)	True	Acute intermittent porphyria	Inferred relationship	Some

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)